UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000049008
Receipt number R000055832
Scientific Title A systematic review and meta-analysis of the usefulness of de-escalation in hospital acquired pneumonia
Date of disclosure of the study information 2022/09/24
Last modified on 2023/03/25 14:21:45

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Basic information

Public title

A systematic review and meta-analysis of the usefulness of de-escalation in hospital acquired pneumonia

Acronym

A systematic review and meta-analysis of the usefulness of de-escalation in hospital acquired pneumonia

Scientific Title

A systematic review and meta-analysis of the usefulness of de-escalation in hospital acquired pneumonia

Scientific Title:Acronym

A systematic review and meta-analysis of the usefulness of de-escalation in hospital acquired pneumonia

Region

Japan


Condition

Condition

hospital-acquired pneumonia

Classification by specialty

Pneumology Infectious disease

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the benefits and harms of de-escalation in the practice of hospital-acquired pneumonia.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The cure rate of pneumonia

Key secondary outcomes

Mortality assessed in each study, the rate of readmission, the occurrence of drug-resistant pathogens, duration of hospital stay, the frequency of adverse events, medical expenses.


Base

Study type

Others,meta-analysis etc


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients with hospital-acquired pneumonia are defined by the 2017 JRS guidelines or hospital-acquired pneumonia is defined by the 2016 ATS/IDSA guidelines.

Key exclusion criteria

Pediatric patients

Target sample size



Research contact person

Name of lead principal investigator

1st name Naoki
Middle name
Last name Iwanaga

Organization

Nagasaki University Hospital

Division name

Department of Respiratory Medicine

Zip code

8528501

Address

Sakamoto 1-7-1, Nagasaki City

TEL

095-819-7273

Email

niwanaga@nagasaki-u.ac.jp


Public contact

Name of contact person

1st name Naoki
Middle name
Last name Iwanaga

Organization

Nagasaki University Hospital

Division name

Department of Respiratory Medicine

Zip code

8528501

Address

Sakamoto 1-7-1, Nagasaki City

TEL

095-819-7273

Homepage URL


Email

niwanaga@nagasaki-u.ac.jp


Sponsor or person

Institute

Systematic review team of Japanese clinical practice guidelines of pneumonia, 2022

Institute

Department

Personal name



Funding Source

Organization

Not applicable

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Not applicable

Address

Not applicable

Tel

Not applicable

Email

Not applicable


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2022 Year 09 Month 24 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Preinitiation

Date of protocol fixation

2022 Year 09 Month 21 Day

Date of IRB


Anticipated trial start date

2022 Year 09 Month 23 Day

Last follow-up date

2022 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

A systematic search of the literature will be conducted in accordance with the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analysis) statement. The Cochrane Central Register of Controlled Trials (CENTRAL), Pubmed, and EMBASE will be used as electronic databases.


Management information

Registered date

2022 Year 09 Month 23 Day

Last modified on

2023 Year 03 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000055832


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name